Abstract: A trial implant system and method of trialling are described. The trial implant system comprises a stem component having a neck including a free end and a neck longitudinal axis. A first trial head has an articulating surface and includes a bore having a bore longitudinal axis and which can receive the free end of the neck with the neck longitudinal axis and bore longitudinal axis coincident. The system includes a first formation and a plurality of second formations angularly disposed around the longitudinal axis. One of the first formation and the plurality of second formations is provided on the neck and the other is provided within the bore. Each of the second formations can matingly engage with the first formation to limit the depth of insertion of the neck into the bore by a different amount.

Abstract: An upper extremity prosthesis may include a prosthetic hand including a prosthetic thumb having a base and a tip, and a prosthetic index finger having a base and a tip. Actuators may be coupled to the upper extremity prosthesis. Prosthetic flexion tendons may have first ends operably coupled to the actuators and second ends coupled to the tips of the thumb and the index finger. Biasing systems may be operably coupled to the prosthetic thumb and the index finger. Upon actuation of the actuators in a first direction, the prosthetic flexion tendons cause the thumb and index finger to flex. Upon actuation of the linear actuators in a second direction opposite the first direction, the biasing systems cause the thumb and index finger to extend.

Abstract: A prosthetic foot device having a longitudinal direction and a transverse direction and comprising a base spring blade, an ankle spring blade being made from a composite material comprising glass fibers and a heel spring blade, the base spring blade and the ankle spring blade being connected in a forefoot region of the prosthetic foot device, the base spring blade and the heel spring blade being connected in a heel region of the prosthetic foot device and the ankle spring blade and the heel spring blade being connected in an ankle region of the prosthetic foot device.

Abstract: The synergetic prosthetic system comprises of a knee and an ankle sleeve on the functional leg and a prosthesis on the amputated leg. Each sleeve comprises of a power supply, an accelerometer, a wireless transmitter and a wire connecting the accelerometer to the wireless transmitter. The prosthesis comprises of a power supply, a microcontroller, servo motors, a knee joint assembly, and an ankle joint assembly. A steel rod covered with a casing connects the knee and ankle joints. The accelerometer measures and transmits the angle of rotation of the functional knee and ankle joint to a microcontroller. The microcontroller pre-programmed with normal gait data pairs the data from the healthy leg and controls the servo motors. The servo motors, move the prosthetic joints to mimic a normal human gait.

Abstract: Hybrid terrain-adaptive lower-extremity apparatus and methods that perform in a variety of different situations by detecting the terrain that is being traversed, and adapting to the detected terrain. In some embodiments, the ability to control the apparatus for each of these situations builds upon five basic capabilities; (1) determining the activity being performed; (2) dynamically controlling the characteristics of the apparatus based on the activity that is being performed; (3) dynamically driving the apparatus based on the activity that is being performed; (4) determining terrain texture irregularities (e.g., how sticky is the terrain, how slippery is the terrain, is the terrain coarse or smooth, does the terrain have any obstructions, such as rocks) and (5) a mechanical design of the apparatus that can respond to the dynamic control and dynamic drive.

Abstract: Prosthetic socket sealing systems and methods of use. Embodiments of the present invention include various combinations of sealing elements that are associated with a rigid prosthetic socket and act to seal the socket interior against air intrusion or escape via the open proximal end thereof. The socket interior may thus be evacuated for purposes of vacuum suspension or otherwise.

Abstract: A stent assembly includes a framework having a tubular rest shape that defines a longitudinal axis, has an external surface that defines an expanded perimeter, and an internal surface that defines a passageway. The framework has a folded shape with a cross section perpendicular to the longitudinal axis that fits in a closed shape having a perimeter that is smaller than the expanded perimeter. The stent assembly has a constrained configuration characterized by the framework being held in the folded shape by a trigger wire supporting sheer stress by being in contact with interlaced loops of the framework. The stent assembly has an unconstrained configuration characterized by the framework being in the tubular rest shape with the trigger wire out of contact with the framework.

Abstract: A stent is disclosed that has an elongated body composed of a bioabsorbable polymer having a proximal end, a distal end, two open spiral channels formed on the exterior surface of the body to provide fluid communication between the proximal end and the distal end. The stent has a central lumen open at the proximal and distal ends of the stent for the passage of a guide wire. The stent also has an anti-migration device used for immobilization of the stent at the target site.

Abstract: Disclosed herein is a stent which includes stent ring structures made up of at least one wire and at least one tubular connector through which a portion of the wire is disposed. The tubular connector includes a side wall with an aperture formed therethrough. A portion of the wire extends therethrough and acts as a barb. A method of making such a stent is also disclosed.

Abstract: An anchor stent assembly to be used with a valve component includes a generally tubular frame having a first end and a second end, the frame defining a central passage and a central axis. A secondary passage is defined between n inner surface of the frame and an outer surface of an inner rib disposed closer to the central axis than the frame. An extension tube is disposed through the secondary passage. The extension tube includes an extension tube lumen having a first opening at a first end of the extension tube and a second opening at a second end of the extension tube.

Abstract: A multilayer bioresorbable stent having sustained drug delivery is disclosed herein. The bioresorbable stent releases a therapeutic substance from the body of the bioresorbable stent starting when the bioresorbable stent is implanted within an anatomical lumen and ending when the entire mass of the bioresorbable stent is no longer present within the anatomical lumen. The bioresorbable stent releases the therapeutic substance gradually during the treatment as the mass of the each layer of the bioresorbable stent erodes. Methods of making the therapeutic layers within the bioresorbable sent are further disclosed. Sustained drug delivery reduces the risk of late and very late stent thrombosis.

Abstract: Stent delivery systems as well as methods for making and using stent delivery systems are disclosed. An example stent delivery system may include an elongate shaft including an inner member having a stent receiving region and a deployment sheath slidably disposed along the inner member. A handle may be coupled to the elongate shaft. A rack member may be coupled to the deployment sheath. At least a portion of the rack member may be designed to extend within the handle. The rack member may include a base portion and a displaceable portion that is displaceable relative to the base portion.

Abstract: An endoluminal delivery device assembly is disclosed. The assembly comprises: an introducer including a seal housing assembly, housing a seal, and an sheath extending proximally therefrom; a delivery device including a handle body and a pusher catheter extending from the body, the pusher catheter having a pusher catheter external surface, the pusher catheter extending through the introducer such that the external surface slideably engages with the seal; a guide wire catheter extending through the body and through the pusher, the guide wire catheter being affixed at a proximal end thereof to a tip assembly; and a linking portion for linking the body and the seal housing assembly together, the linking portion having an unlinked condition and a linked condition. In the linked condition, sliding movement between the pusher catheter and the seal is limited such that disengagement between the pusher catheter external surface and the seal is prevented.

Abstract: Noninvasive natural healing in daily life or regenerative cell treatment can be promoted. A knee joint model is constructed by three-dimensionally analyzing measurement data obtained by measuring an outline shape and internal space shape of a knee joint part of a subject; a transition state towards an orthotic direction for a symptom improvement of the knee joint part is simulated continuously or stepwisely with reference to the knee joint model; and an exoskeleton mold capable of continuously or stepwisely finely adjusting the knee joint part towards the orthotic direction is designed based on the transition state.

Abstract: In combination with a knee brace, the variable radius spring assembly of the present invention provides a full range knee orthotic with support to the leg muscles without compromising the range of motion and the patient's normal walk/gate. The assembly comprises upper and lower hinge pieces attached to upper and lower sections of the brace, a spring bracket, and an elongated spring element that extends downward from the upper hinge piece past a catch on the lower hinge piece. Two such assemblies are attached to a knee brace, one on the inner side and one on the outer side. As the lower leg, and the lower hinge piece, move rearward, the catch forces the spring element rearward and slides downward along the spring element. Consequently, the spring element has a non-linear response requiring approximately the same about of force to deflect the spring element throughout its range of rearward travel.

Abstract: Devices and methods for treating penile aberrations include the use of traction devices. For example, this document describes devices and methods for applying longitudinal and/or contralateral penile traction forces to treat anatomical aberrations related to Peyronie's disease and other conditions.

Abstract: A personal urinary device for a female has a straight, round tube of biodegradable material, having one end exhibiting an angle with a plane perpendicular to an axis of the tube, a lip having a diameter larger than the outside diameter of the tube, on the outside of the tube at a first distance from an end opposite the angled end, and a rounded element at the end opposite the angled end.

Abstract: An oral appliance device that selectively engages upper teeth and lower teeth within a human mouth includes an upper appliance member, a lower appliance member, and a first vertical shim. The upper appliance member selectively engages the upper teeth. The lower appliance member selectively engages the lower teeth. The appliance members are movable relative to one another between an open position and a closed position. The first vertical shim is removably secured to one of the appliance members. The first vertical shim has a first shim height so that a teeth spacing between the upper teeth and the lower teeth is maintained when the appliance members are in the closed position. The teeth spacing is at least as great as the first shim height. The oral appliance device can further include a second vertical shim that is alternatively, removably secured to one of the appliance members. The second vertical shim has a second shim height that is different than the first shim height.

Abstract: An oral appliance device for use within a human mouth includes an upper appliance member, a lower appliance member, and a connector assembly. The upper appliance member selectively engages upper teeth within the human mouth. The lower appliance member selectively engages lower teeth within the human mouth. The connector assembly movably connects the upper appliance member and the lower appliance member to one another. The connector assembly includes a first connector button that is removably secured to the upper appliance member, a second connector button that is removably secured to the lower appliance member, and a connector band that is coupled to the upper appliance member with the first connector button and coupled to the lower appliance member with the second connector button.

Abstract: An oral appliance device for use within a human mouth includes an appliance member and a nasal dilator assembly. The appliance member selectively engages teeth within the human mouth. The nasal dilator assembly is configured to dilate a nasal passage when positioned entirely within the human mouth. Additionally, the nasal dilator assembly includes a first nasal dilator that is removably coupled to the appliance member. The nasal dilator assembly can further include a dilator receiver that is integrally formed with the appliance member. At least a portion of the first nasal dilator can be removably received and retained within the dilator receiver so that the first nasal dilator is removably coupled to the appliance member.

Abstract: A female condom includes a base section composed of elastic silicon that tends to hold shape. The base section is sized to remain on the outside of a vaginal cavity. The base section includes a hole. A tubular section is attached to the base section. The tubular section is designed to fit within the vaginal cavity. The tubular section is situated on the base section to entry through the hole in the base section to the tubular section. The tubular section is composed of medical grade silicon. The tubular section includes a tube infrastructure. The tube infrastructure is composed of silicon that is flexible but is of sufficient elasticity and resilience that the tube infrastructure tends to hold the tubular section of the female condom in an expanded state.

Abstract: A system for cooling the brain of a human subject, the system including a cooling subsystem configured to input a flow of air or breathable gas, cool the air or breathable gas, and output cooled air or breathable gas to a line coupled to a device adapted to deliver the cooled air or breathable gas to a human subject. A flow control device coupled to the cooling subsystem is configured to control a flow rate of the flow of the air or breathable gas input to the cooling subsystem and a flow rate of the cooled air or breathable gas output to the line. One or more flow rate sensors coupled to the cooling subsystem are configured to measure at least a flow rate of flow of cooled air or breathable gas. One or more temperature sensors are configured to measure at least a temperature of a brain or a brain correlative site of the human subject and the temperature of the flow of cooled air or breathable gas.

Abstract: A self-heating warming blanket includes a pliable outer shell forming a liquid impermeable enclosure. A heat generation layer disposed inside the enclosure has a plurality of liquid permeable heater compartments containing an exothermic reactant. The blanket also has a heater activation system including a sealed bladder containing an activator liquid inside the enclosure. An activation strip extends from outside the outer shell into the enclosure. One segment of the strip is an unsealing segment connected to the bladder. Another segment of the strip is a handle segment outside the outer shell. Pulling on the handle segment opens the bladder and releases the activator liquid into the enclosure where at least a portion of it permeates at least one heater compartment and combines with the exothermic reactant contained therein to initiate an exothermic chemical reaction that heats the warming blanket.

Abstract: Various embodiments of the present disclosure provide a device for cooling tissue comprising a tube having an inlet end and an outlet end opposite the inlet end and an interior traversing the length of the tube, the interior being a passageway for cooling fluid to circulate within the interior; wherein the tube is shaped to a contour of biological tissue of a patient. Other embodiments provide a method for cooling tissue comprising applying a tubular contact cooler to a patient's tissue configured to circulate a cooling fluid through the interior of the contact cooler; wherein the cooling fluid's temperature is below 14° Celsius and the contact cooler is shaped to a contour of tissue.

Abstract: A catheter is provided comprising a flexible heat transfer element provided on an outer surface of the catheter, a conduit arranged to supply an inflation fluid for inflating the flexible heat transfer element so as to form an inflated balloon, a guide wire lumen for receiving a guide wire, and an elongate cooling element arranged to cool said inflation fluid for inflating the balloon. Said cooling element and said guide wire lumen are arranged inside the flexible heat transfer element such that, when inflated the cooling element is substantially central within the balloon and said guide wire lumen is parallel to and radially offset from the cooling element.

Abstract: A method of manufacturing a surgical device can include generating a first internal frame defining an internal structure of an instrument tip; covering at least a portion of the first internal frame with a first coating to define an exterior surface of the instrument tip; and generating an instrument body such that a proximal end of the instrument tip is positioned at a distal end of the instrument body. An ophthalmic surgical instrument can include an instrument body; and an instrument tip disposed at a distal end of the instrument body, the instrument tip including a first section linearly extending along a longitudinal axis of the instrument body and a second section extending obliquely from the first section, the second section being arcuately shaped; and wherein the instrument tip comprises a first internal frame and a first coating covering the first internal frame.

Abstract: Board-like forceps for ophthalmic use comprise forceps handles and forceps boards. The forceps handles comprise an upper forceps handle (1) and a lower forceps handle (2), two ends of which are connected to form a V-type structure. The length of the lower forceps handle (2) is greater than that of the upper forceps handle (1). An upper forceps board (3) and a lower forceps board (4) having a same shape are correspondingly disposed on unconnected ends of the upper forceps handle (1) and the lower forceps handle (2), and are bent in a same side direction. An included angle formed by the upper forceps board (3) and the upper forceps handle (1) is smaller than an included angle formed by the lower forceps board (4) and the lower forceps handle (2).

Abstract: A mirror for an ophthalmic laser treatment device that is movable on an axis from a position in a treatment laser beam path to a position out of the treatment laser beam path. The mirror reflects light from a light source into the eye of a patient. The mirror is biased towards a position in the path and is moved out of the path by an actuator just long enough for the laser treatment to be applied and without noticeable interruption to viewing by a user.

Abstract: Provided herein is a probe for treating an eye of a patient. In one or more embodiments, the probe includes a body, and a tubular element having a main lumen extending from the body, the tubular element comprising a distal end. The probe further includes a visualization optical fiber within the main lumen, the visualization optical fiber adapted to emit an illumination provided by at least one of a plurality of light sources connected to the visualization optical fiber. In some embodiments, the probe further includes an optical switching system (e.g., a time-division multiplexor) operable with the plurality of light sources, wherein the optical switching system is adapted to independently control each of the plurality of light sources. By providing time-division multiplexing between different surgical light sources, quasi-simultaneous illumination delivery through the same optical path may be achieved.

Abstract: An instrument for removing debris from an eye during the treatment of an ocular disorder has a swab and a rigid member. The swab includes a tip portion sized to provide access to the debris on an eyelid of the eye. The rigid member has a distal end portion affixed to the swab and a proximal end portion with a cross-sectional member profile. The cross-sectional member profile is non-circular and has a first groove. The first groove extends longitudinally along the proximal end portion for cooperating with a chuck such that rotation of the proximal end portion within the chuck is inhibited.

Abstract: A work tip for a surgical hand piece has a solid blade connected to a source of ultrasonic energy in the hand piece. The knife has grooves in its surfaces. The work tip further including an irrigation and aspiration tubes extending along opposite surfaces of the blade and being at least partially within the grooves. The blade has a collar adjacent its distal end and at least the aspiration tube extends ends at a distance from the collar. The edges of the collar are made sharp enough to emulsify cataract tissue when vibrated at ultrasonic frequencies so that occlusion of the aspiration tube is prevented.

Abstract: A device and method for cutting or ablating tissue in a human or veterinary patient includes an elongate probe having a distal end, a tissue cutting or ablating apparatus located adjacent within the distal end, and a tissue protector extending from the distal end. The protector generally has a first side and a second side and the tissue cutting or ablating apparatus is located adjacent to the first side thereof. The distal end is structured to be advanceable into tissue or otherwise placed and positioned within the patient's body such that tissue adjacent to the first side of the protector is cut away or ablated by the tissue cutting or ablation apparatus while tissue that is adjacent to the second side of the protector is not substantially damaged by the tissue cutting or ablating apparatus.

Abstract: A device and a method for using laser energy for treatment of tissue, which can include generating short bursts of energy at a range of pulse repetition rates. The method comprises selective surface and/or three-dimensional interactions for therapeutic use and/or to modify or remove tissue from targets. The device and method can subsurface disruptions in tissue at selected depths and densities.

Abstract: A method is described of improving adhesion of an ocular implant to corneal tissue by forming an implant adhesive layer on the ocular implant, the implant adhesive layer having greater adhesive strength than a rest of the implant or by forming a corneal adhesive layer on a posterior surface of a posterior portion of the corneal tissue, the corneal adhesive layer having greater adhesive strength than a rest of the corneal tissue.

Abstract: Laser assisted cataract surgery methods and devices utilize one or more treatment laser beams to create a shaped opening in the anterior lens capsule of the eye when performing a capsulorrhexis procedure. A light absorbing agent may be applied to the anterior lens capsule to facilitate laser thermal separation of tissue along a treatment beam path on the lens capsule. Relative or absolute reflectance from the eye, and optionally from a surgical contact lens, may be measured to confirm and optionally quantify the presence of the light absorbing agent, before the treatment beam is applied.

Abstract: A treatment device for the surgical correction of defective vision in an eye. The device includes a laser apparatus controlled by a controller. The controller determines a desired correction of defective vision from measurement data of the eye to produce control data for the laser, and to control the laser to emit radiation according to the control data, such that a lenticule-shaped volume is isolated in the cornea. The controller computes a lenticule-shaped intended volume, the removal of which from the cornea leads to an actual correction of defective vision in an optical zone in the eye which differs from the desired correction more at the edge of the optical zone than at the center of the optical zone. The thickness of the lenticule-shaped intended volume is less than the thickness of a lenticule-shaped comparison volume, the removal of which would bring about the desired correction of defective vision.

Abstract: The invention relates to an apparatus for changing the refractive power of the cornea (1), in particular for correcting hyperopia or presbyopia, exhibiting injection means (13, 15) having at least one hollow needle (15) for injecting at least one optically transparent filling material having a predetermined refractive index into an intrastromal corneal pocket (7), characterized by a controllable injection drive (17) that is coupled at least indirectly to the injection means (13, 15) and is designed for changing an amount, to be injected, of the at least one filling material; a device for optical coherence tomography (OCT) (19) that is designed for monitoring the area of the corneal pocket (7) by means of measurement of depth profiles of the cornea (1) on a repeatedly cycled-through scan pattern; and a computing unit (21) that is designed and/or configured to determine from the measurement data of the OCT device (19) at least the radius of curvature of the front (3) of the cornea (1) keeping pace temporally wi

Abstract: An emergency head trauma bandage cap with a detachable strap system and method of use, which, when applied to the head, delivers minimal pressure to control bleeding, doesn't compromise cervical spine immobilization, allows for fast and effective application of cooling gel to control intracranial/internal swelling or hot packs to prevent hypothermia in non-trauma situations, doesn't come apart during treatment and transport, and doesn't require a caregiver to re-wrap the dressing.

Abstract: A dressing may comprise a backing layer having an interior region and a border region around the interior region. A dermal interface may be disposed in the border region. The dermal interface may comprise an adhesive and a therapeutic composition, such as a topical analgesic. The therapeutic composition may be dissolved into the adhesive, and preferably constitutes at least 20 percent of the dermal interface. In some embodiments, the therapeutic composition may comprise at least 30 percent of the dermal interface.

Abstract: Methods and apparatuses are disclosed relating to the creation and use of bespoke wound fillers and other wound treatment apparatuses. Some embodiments provide for the creation of bespoke wound fillers based on characteristics of a wound. Certain embodiments also include the use of bespoke wound fillers in combination with negative pressure to treat a wound.

Abstract: Wound contacting members and methods, apparatuses, systems and kits incorporating the same are disclosed. The wound contacting members offer improved performance in terms of preventing or inhibiting tissue in-growth and improving tissue granulation growth. The wound contacting members may be used in negative pressure wound therapy (NPWT) applications.

Abstract: An orthopedic splint system comprising self curing splinting system that is applied to an injured limb without use of water. The splint material is contained in tear resistant outer pouch and an inner protective sleeve where a water-laden gel is contained in a pouch situated in direct contact with the splint material. Said liquid pouch will be torn when a longitudinal tab, which is an integral part of the pouch, is pulled out releasing the water-laden gel which will come in contact with the splint system causing it to cure.

Abstract: The present invention is a weather-resistant cover for a walking brace, cast, and/or orthotic device used on a human leg and foot. This innovative cover includes a sturdy, slip-resistant outer sole for safe mobility. The majority of the protective cover is comprised of a flexible, resilient, and weather-resistant material. In contrast, patches of flexible, thin fabric are present over the regulatory buttons of the walking brace, cast, and/or orthotic device. These patches allow for the fitting of the walking brace, cast, or orthotic device to be adjusted while the cover is in use. A drawstring is present at the top of the cover to ensure the cover is completely weather-resistant. This cover also includes a longitudinal fastener at the rear of the cover to allow the wearer to easily place their leg/foot in the device. This fastener, when closed, secures the wearer's appendage in the cover.

Abstract: A compression garment comprises an elongated stretchable sleeve (1) which is adapted to be worn over a body part and a compression part (2) connected to the elongated stretchable sleeve (1). The garment has at least one closing part (3) for fixing the compression part (2) in a stretched state. Furthermore, the compression part (2) is shaped and sized to be wrapped around the circumference of the elongated stretchable sleeve (1), wherein the compression part (2) is adapted for positioning proximate to an outer surface of the elongated stretchable sleeve (1).

Abstract: A therapeutic pressure band for applying pressure across a muscle or muscle groups on a mammalian limb is described. The band is particularly well suited for treating “shin splints.” The band includes a plurality of straps that are connected together via a connecting material. Ends of each of the straps have adjustable fasteners for securing and tightening the band around a limb. The band also possesses a plurality of pressure members (e.g., elongated rubber tubes) that apply separate and discrete areas or points of pressure in a line across a muscle, tendon, bone, or muscle group and generally perpendicular to a longitudinal axis of the limb.

Abstract: The invention relates to a unit for hemostasis. The unit is configured to be directly applied to a bleeding wound and comprises an envelope enclosing an inner space as well as an effective amount of a hemostatic material disposed within the inner space. Furthermore, the invention relates to an arrangement of two or more such units for hemostasis, the units being coupled to each other. Moreover, the invention relates to a method for producing an arrangement of units for hemostasis. In accordance with the method, an effective amount of a hemostatic material is disposed within an interior region of a starting material, and neck regions are formed on both sides of the charge so as to form an envelope enclosing the charge.

Abstract: A nose cleaning swab system including a cleaning swab having a handle and an auger swab head. The auger swab head has a swirled profile including a plurality of spaced ribs. As a user twists the handle, the auger swab head efficiently removes material out of a bodily orifice when the auger swab head is inserted into the bodily orifice such as a nose. The auger swab head is tapered from a tip to a base where the auger swab head is connected to the handle creating a continuous one-piece the cleaning swab.

Abstract: A moisture management apparatus monitors an area for moisture events and wirelessly transmits moisture-related information to one or more notification devices. An embodiment of the moisture management apparatus includes a substrate and one or more sensors supported by the substrate. The sensor(s) emit wireless signals indicative of the moisture-related information. A sensor event communication system forwards the sensor signals to another device, such as a notification device. The sensor event communication system may monitor other types of patient events. Portions of the moisture management apparatus and/or the moisture event communication system may be embodied in a patient support apparatus, such as a bed.

Abstract: Absorbent articles with front and rear opening features are disclosed. An article may comprise an insert comprising an outer cover, a liner, and a core between the outer cover and liner, a first waist panel coupled to the insert throughout a first attachment region, and a second waist panel coupled to the insert throughout a second attachment region, the second panel being coupled to the first panel proximate a first side edge of the article and the second side edge of the article and further comprising a weakened region. The second attachment may comprise a low-strength attachment zone and a high-strength attachment zone, the high-strength attachment zone disposed proximate the attachment region bottom edge. The low-strength attachment zone may further have a first peel strength and the high-strength attachment zone may have a second peel strength, the second peel strength greater than the first.

Abstract: In an underpants-type disposable diaper, three-dimensional gathers are provided on both sides in the width direction of an inner member. A fallen portion of each of the three-dimensional gather has a fallen non-stretchable portion to which a contraction force of gather elastic members does not act. A character representation is printed at a position in the fallen non-stretchable portion of the inner member, and this character representation is made visible from the inside of the diaper.